Department of Surgery, Nagasaki University Graduate School of Biomedical Sciences/Nagasaki University Hospital, Nagasaki, Japan.
Atopy (Allergy) Research Center, Juntendo University, Tokyo, Japan.
Transplant Proc. 2021 Oct;53(8):2570-2575. doi: 10.1016/j.transproceed.2021.08.026. Epub 2021 Sep 10.
We report on the case of a 50-year-old female patient with symptomatic polycystic liver disease who underwent living donor liver transplantation (LDLT) using right liver graft from her ABO-identical husband. To achieve operational tolerance, regulatory T-cell (T-reg)-based cell therapy was applied, following the protocol introduced by Todo et al. Briefly, donor lymphocytes were collected by leukapheresis 20 days before LDLT without any adverse events, and the cells were irradiated with a dose of 30 Gy and kept frozen. Lymphopheresis of the recipient was conducted in a similar manner 1 day before LDLT, and donor cells and recipient cells were cultured with anti-CD80/86 antibodies to induce the donor-specific T-reg. At 14 days of culture, the CD4CD25Foxp3 cells had increased from 1.51% to 5.21%, and mixed lymphocyte reaction assay using an intracellular fluorescent dye carboxyfluorescein diacetate succinimidyl ester-labeling technique revealed donor-specific hyporesponsiveness of CD4-positive lymphocytes. On postoperative day (POD) 13 (14 days of culture), these cells were infused to the recipient intravenously without any adverse events. Initial immunosuppression consisted of tacrolimus, steroid and mycophenolate mofetil (MMF), and cyclophosphamide (40 mg/kg) administered on POD 5. Both the steroid and MMF were continued until 4 weeks after LDLT, and the patient was discharged on POD 30 with normal liver function. On POD 52, the patient developed acute cellular rejection and received appropriate reinforcement of immunosuppressive therapy and is currently doing well with normal liver function 30 months after LDLT with reduced anti-donor allo-activity. In summary, T-reg therapy was safely performed in adult LDLT, and we are following the patient carefully to determine whether she can achieve operational tolerance in the future.
我们报告了一例 50 岁女性多囊肝病患者,接受了来自其 ABO 同型丈夫的右半肝供体进行活体肝移植(LDLT)。为了实现免疫耐受,采用了基于调节性 T 细胞(T-reg)的细胞治疗,该方案是基于 Todo 等人的介绍。简要地说,在 LDLT 前 20 天,通过白细胞分离术采集供者淋巴细胞,无任何不良反应,然后用 30Gy 的剂量照射并冷冻保存细胞。在 LDLT 前 1 天,以类似的方式对受者进行淋巴细胞分离,并用抗 CD80/86 抗体培养供者细胞和受者细胞,以诱导供者特异性 T-reg。在培养的第 14 天,CD4CD25Foxp3 细胞从 1.51%增加到 5.21%,并且使用细胞内荧光染料羧基荧光素二乙酸琥珀酰亚胺酯标记技术的混合淋巴细胞反应测定显示 CD4 阳性淋巴细胞的供者特异性低反应性。在术后第 13 天(培养的第 14 天),这些细胞无不良反应地静脉输注给受者。初始免疫抑制方案包括在术后第 5 天给予他克莫司、类固醇和霉酚酸酯(MMF)以及环磷酰胺(40mg/kg)。类固醇和 MMF 一直持续到 LDLT 后 4 周,受者在术后 30 天出院,肝功能正常。在 LDLT 后 52 天,患者发生急性细胞排斥反应,给予适当的免疫抑制治疗强化,目前在 LDLT 后 30 个月肝功能正常,并且对供者同种异体反应性降低。总之,T-reg 治疗在成人 LDLT 中安全进行,我们正在密切随访患者,以确定她是否能在未来实现免疫耐受。